0000000001312547

AUTHOR

Anja Schüffler

showing 26 related works from this author

Isolation, structure elucidation, and biological evaluation of the unusual heterodimer chrysoxanthone from the ascomycete IBWF11-95A

2009

Chrysoxanthone, an unusual heterodimer of blennolide A and 2-hydroxychrysophanol linked through a diaryl ether bridge, was isolated from mycelia of the ascomycete IBWF11-95A grown in submerged culture. Its structure was elucidated by two-dimensional NMR spectroscopy. The metabolite shows antibacterial activity against different species with MIC values between 2.5 and 20 μg/mL while also inhibiting the growth of several fungi.

Diaryl etherStereochemistryMetaboliteOrganic ChemistryNuclear magnetic resonance spectroscopyIsolation (microbiology)Biochemistrychemistry.chemical_compoundchemistryMic valuesDrug DiscoveryAntibacterial activityMyceliumBiological evaluationTetrahedron Letters
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Erysacleuxins C and D, new isoflavones from the twigs of Erythrina sacleuxii Hua and their cytotoxic activity

2020

Two previously undescribed isoflavones, erysacleuxin C (1) and erysacleuxin D (2), together with seven known compounds (3–9), were isolated and identified from the EtOAc extract of the twigs of Erythrina sacleuxii Hua (Leguminosae). The structures of the isolated compounds were determined on the basis of their spectroscopic and spectrometric data. Evaluation of their cytotoxicity against the human cancer HeLa-S3 cell lines indicated IC50 values of 130.4, 54.9 and 73.9 µM for erysacleuxin C (1), erysacleuxin D (2) and butin (9), respectively. Keywords: Erythrina sacleuxii, Leguminosae, Isoflavone, Erysacleuxin C, Erysacleuxin D, Cytotoxicity

ButinTraditional medicinebiologyGeneral Chemical Engineering02 engineering and technologyGeneral ChemistryIsoflavones010402 general chemistry021001 nanoscience & nanotechnologybiology.organism_classification01 natural sciences0104 chemical scienceslcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999Cell cultureIc50 valuesCytotoxic T cellErythrina sacleuxii0210 nano-technologyCytotoxicityHuman cancerArabian Journal of Chemistry
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Identification of Patulin from Penicillium coprobium as a Toxin for Enteric Neurons

2019

The identification and characterization of fungal commensals of the human gut (the mycobiota) is ongoing, and the effects of their various secondary metabolites on the health and disease of the host is a matter of current research. While the neurons of the central nervous system might be affected indirectly by compounds from gut microorganisms, the largest peripheral neuronal network (the enteric nervous system) is located within the gut and is exposed directly to such metabolites. We analyzed 320 fungal extracts and their effect on the viability of a human neuronal cell line (SH-SY5Y), as well as their effects on the viability and functionality of the most effective compound on primary ent…

Central nervous systemPharmaceutical SciencemicrobiomeBiologymedicine.disease_causeAnalytical ChemistryMicrobiologyPatulinlcsh:QD241-44103 medical and health sciencesPolyketidechemistry.chemical_compound0404 agricultural biotechnologyenteric nervous systemlcsh:Organic chemistrymycotoxinsDrug DiscoverymedicineMicrobiomePhysical and Theoretical Chemistryfusarium030304 developmental biologyCalcium signaling0303 health sciencesToxinOrganic Chemistry04 agricultural and veterinary sciences040401 food science<i>Penicillium</i>medicine.anatomical_structurechemistryChemistry (miscellaneous)Cell cultureMolecular Medicinegastrointestinal systemEnteric nervous systemfungiMolecules
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Tanzawaic acids I-L: Four new polyketides from Penicillium sp. IBWF104-06.

2014

Four new polyketides have been identified in culture filtrates of the fungal strain Penicillium sp. IBWF104-06 isolated from a soil sample. They are structurally based on the same trans-decalinpentanoic acid skeleton as tanzawaic acids A–H. One of the new compounds was found to inhibit the conidial germination in the rice blast fungus Magnaporthe oryzae at concentrations of 25 μg/mL.

biologyChemistrynatural productsOrganic Chemistrystructure elucidationfood and beveragesFungusbiology.organism_classificationFull Research PaperarohynapeneMicrobiologylcsh:QD241-441Magnaporthe oryzaeChemistrylcsh:Organic chemistryGerminationPenicilliumtanzawaic acidFungal strainlcsh:Qlcsh:SciencepolyketidesBeilstein journal of organic chemistry
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Back Cover: Promoter Activation in Δ hfq Mutants as an Efficient Tool for Specialized Metabolite Production Enabling Direct Bioactivity Testing (Ange…

2019

chemistry.chemical_compoundbiologyBiochemistryChemistryMetaboliteMutantINTCover (algebra)General ChemistryProteobacteriabiology.organism_classificationCatalysisAngewandte Chemie International Edition
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Prenylated isoflavones from the stem bark of Erythrina sacleuxii

2018

Abstract Two new prenylated isoflavones, named erysacleuxin A (1) and B (2), along with eight known compounds, biochanin A (3), 5′-(3-methylbut-2-enyl)pratensein (4), 7-demethylrobustigenin (5), 3′-(3-methylbut-2-enyl)biochanin A (6) abyssinone V-4′-methyl ether (7), sigmoidin E (8), erythrinasinate (9), and burtinone (10) were isolated from the stem bark of Erythrina sacleuxii Hua (Leguminosae). The structures were determined based on spectroscopic and spectrometric data. All isolated compounds were evaluated for antifungal activity against Botrytis cinerea, Candida albicans, Eremothecium coryli, Penicillium notatum, Pyricularia oryzae, and Rhizomucor miehei with compounds 3, 4 and 6 showi…

Eremothecium corylibiologyTraditional medicine010405 organic chemistryRhizomucor mieheiPratenseinPlant ScienceIsoflavonesbiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesBiochanin A010404 medicinal & biomolecular chemistrychemistry.chemical_compoundchemistryPenicilliumErythrina sacleuxiiAgronomy and Crop ScienceBiotechnologyBotrytis cinereaPhytochemistry Letters
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Isolactarane and Sterpurane Sesquiterpenoids from the Basidiomycete Phlebia uda

2012

Three new sesquiterpenoids, named udasterpurenol A, udalactarane A, and udalactarane B, as well as the known compounds hyphodontal and sterpuric acid have been isolated from the basidiomycete Phlebia uda. These compounds represent the first natural products described from this species. The structures were elucidated by NMR spectroscopy and mass spectrometry. Udalactaranes A and B were isolated as mixtures with their respective epimeric acetals. These mixtures inhibited the spore germination of the plant pathogenic fungus Fusarium graminearum at 10 and 5 μg/mL, respectively, and were active against Jurkat cells with IC(50) values of 101 and 42 μM, respectively.

FusariumStereochemistryPharmaceutical ScienceMicrobial Sensitivity TestsMass spectrometryAnalytical ChemistryInhibitory Concentration 50Jurkat CellsFusariumDrug DiscoveryIc50 valuesSpore germinationHumansNuclear Magnetic Resonance BiomolecularPharmacologyMolecular StructurebiologyBasidiomycotaOrganic ChemistryBasidiomycotaNuclear magnetic resonance spectroscopyPathogenic fungusbiology.organism_classificationPhlebia udaComplementary and alternative medicineMolecular MedicineSesquiterpenesJournal of Natural Products
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Elucidation of the biosynthesis and degradation of allantofuranone by isotopic labelling and fermentation of modified precursors.

2010

Feeding experiments with the ascomycete Allantophomopsis lycopodina indicated that the potent fungistatic allantofuranone is biosynthesized from phenylalanine. Further experiments with synthetic precursors gave evidence that the naturally occurring polyporic acid serves as a key intermediate in the biosynthesis. In addition to the formation of allantofuranone, its abiotic and metabolic degradation were investigated.

Abiotic componentAntifungal AgentsOrganic ChemistryFungiPolyporic acidPhenylalanineBiologyBiochemistryIsotopic labelingchemistry.chemical_compoundBiosynthesischemistryBiochemistry4-ButyrolactoneLabellingIsotope LabelingFermentationMolecular MedicineDegradation (geology)FermentationMolecular BiologyChembiochem : a European journal of chemical biology
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Chemical constituents of the root wood of Erythrina sacleuxii and determination of the absolute configuration of suberectin

2020

Phytochemical investigation on the root wood of Erythrina sacleuxii (Leguminosae) led to the isolation of nine secondary metabolites (1-9). Compound 1 was isolated from the genus Erythrina for the first time. The pure compounds were identified on the basis of comprehensive spectroscopic and spectrometric analyses, while their absolute configurations were determined based on chiroptical measurements. Compounds 5 and 6 showed weak antifungal activity against Pyricularia oryzae with MIC values of 20 µg/mL.&#x0D;  &#x0D; Bull. Chem. Soc. Ethiop. 2020, 34(1), 135-140.&#x0D; DOI: https://dx.doi.org/10.4314/bcse.v34i1.12

AntifungalPyriculariabiologymedicine.drug_classChemistryAbsolute configurationGeneral Chemistry010402 general chemistrybiology.organism_classification01 natural sciences0104 chemical sciencesPhytochemicalMic valuesChemical constituentsmedicineErythrina sacleuxiiErythrinaNuclear chemistryBulletin of the Chemical Society of Ethiopia
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Anti-phytopathogen terpenoid glycosides from the root bark of Chytranthus macrobotrys and Radlkofera calodendron

2020

Abstract Chytranthus macrobotrys and Radlkofera calodendron are two Sapindaceae characterized by a lack of phytochemical data. Both root barks from the two Sapindaceae species were processed by ethanol extraction followed by the isolation of their primary constituents by liquid chromatography. This process yielded four previously undescribed terpenoid glycosides together with eight known analogues. Extracts and isolated compounds from C. macrobotrys and R. calodendron were then screened for antimicrobial activity against fifteen phytopathogens. The biological screening also involved extracts and pure compounds from Blighia unijugata and Blighia welwitschii, two Sapindaceae previously studie…

0106 biological sciencesPyriculariaFomitiporia mediterraneaPlant SciencePhaeomoniella chlamydosporaHorticultureSapindaceaeXylella01 natural sciencesBiochemistryRhizoctoniaRhizoctonia solaniSapindaceaeAscomycotaFusariumFusarium oxysporumBotanyGlycosidesPythiumMolecular BiologyBotrytis cinereabiologyPlant ExtractsTerpenes010405 organic chemistrybiology.plant_disease_causeBasidiomycotaGeneral MedicineSaponinsbiology.organism_classification0104 chemical sciencesPlant BarkBotrytis010606 plant biology & botanyPhytochemistry
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Hirsutane-Type Sesquiterpenes with Uncommon Modifications from Three Basidiomycetes

2010

From three basidiomycetes, Xeromphalina sp., Stereum sp., and Pleurocybella porrigens, six triquinane sesquiterpenes with unprecendented modifications and a rearranged sesquiterpene related to coriolin C have been isolated. Their isolation, structure elucidation, and biological evaluation are described.

Bridged-Ring CompoundsPolycyclic SesquiterpenesAntifungal AgentsBacteriaMolecular StructurebiologyStereochemistryXeromphalinaBasidiomycotaOrganic ChemistryFungibiology.organism_classificationSesquiterpenePleurocybella porrigensTerpenoidAnti-Bacterial Agentschemistry.chemical_compoundchemistryOrganic chemistryStereumSesquiterpenesBiological evaluationThe Journal of Organic Chemistry
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Phosphorylation and activation of endothelial nitric oxide synthase by red fruit (Pandanus conoideus Lam) oil and its fractions

2020

Abstract: Ethnopharmacological relevance Red fruit (Pandanus conoideus Lam) oil (RFO) is utilized by inhabitants of the Papua Island to treat diseases such as infections, cancer, and cardiovascular disease, but the mechanism of action is unknown. Aim of the study We have recently shown that RFO stimulates nitric oxide (NO) production in endothelial cells. The present study was conducted to investigate the molecular mechanism of endothelial NO synthase (eNOS) activation by RFO. Materials and methods NO production by endothelial cells was determined with electron paramagnetic resonance. The vascular function of isolated mouse aorta was examined using a wire myograph system. Phosphorylation of…

Nitric Oxide Synthase Type IIIVasodilator AgentsAorta ThoracicVasodilationPharmacologyNitric OxideCell LineNitric oxide03 medical and health scienceschemistry.chemical_compound0302 clinical medicineEnosDrug DiscoverymedicineAnimalsHumansPlant OilsPhosphorylationPandanaceaeProtein kinase BPI3K/AKT/mTOR pathway030304 developmental biologyPharmacology0303 health sciencesbiologyEndothelial CellsAMPKbiology.organism_classificationMice Inbred C57BLchemistryMechanism of actionFruit030220 oncology & carcinogenesisPhosphorylationmedicine.symptomJournal of Ethnopharmacology
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Unravelling the biosynthesis of pyriculol in the rice blast fungus Magnaporthe oryzae

2017

Pyriculol was isolated from the rice blast fungus Magnaporthe oryzae and found to induce lesion formation on rice leaves. These findings suggest that it could be involved in virulence. The gene MoPKS19 was identified to encode a polyketide synthase essential for the production of the polyketide pyriculol in the rice blast fungus M. oryzae. The transcript abundance of MoPKS19 correlates with the biosynthesis rate of pyriculol in a time-dependent manner. Furthermore, gene inactivation of MoPKS19 resulted in a mutant unable to produce pyriculol, pyriculariol and their dihydro derivatives. Inactivation of a putative oxidase-encoding gene MoC19OXR1, which was found to be located in the genome cl…

0106 biological sciences0301 basic medicineMagnaportheMutantSecondary Metabolism01 natural sciencesMicrobiologyMicrobiology03 medical and health sciencesPolyketideGene Expression Regulation FungalPolyketide synthaseAxenicGenePlant DiseasesRegulation of gene expressionbiologyFungal geneticsfood and beveragesOryzabiology.organism_classificationPlant LeavesMagnaporthe030104 developmental biologyBenzaldehydesMultigene FamilyPolyketidesbiology.proteinFatty AlcoholsPolyketide SynthasesTranscription FactorsResearch Article010606 plant biology & botanyMicrobiology
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Neo-clerodane diterpenoids from Conyza pyrrhopappa Sch.Bip. ex A.Rich

2019

Two hitherto unknown neo-clerodane-type diterpenoids along with twelve known compounds have been isolated from Conyza pyrrhopappa Sch.Bip. ex A.Rich, a medicinal plant traditionally used across tropical Africa to relieve fever. The structures of isolates have been elucidated by a combination of spectroscopic techniques. The crude extract and the isolated compounds were evaluated in the Hela-S3 cell line and in a panel of microorganisms (bacteria and fungi) at concentrations up to 50 µg/mL. The new compounds were inactive while the pentamethylated flavonoids showed low to significant activity against the cancer cell line used. However, none of the samples showed any activity against the test…

biologyTraditional medicine010405 organic chemistryChemistryMicroorganismOrganic ChemistryPlant ScienceAsteraceaebiology.organism_classificationAntimicrobialIsolation (microbiology)01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistryCell cultureCancer cell linesCytotoxicityBacteriaNatural Product Research
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Rücktitelbild: Promoter Activation in Δ hfq Mutants as an Efficient Tool for Specialized Metabolite Production Enabling Direct Bioactivity Testing (A…

2019

chemistry.chemical_compoundBiochemistryChemistryMetaboliteMutantGeneral MedicineAngewandte Chemie
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Identification of NF-κB as Determinant of Posttraumatic Stress Disorder and Its Inhibition by the Chinese Herbal Remedy Free and Easy Wanderer

2017

Posttraumatic stress disorder (PTSD) is a mental disorder developing after exposure to traumatic events. Although psychotherapy reveals some therapeutic effectiveness, clinically sustainable cure is still uncertain. Some Chinese herbal formulae are reported to work well clinically against mental diseases in Asian countries, but the safety and their mode of action are still unclear. In this study, we investigated the mechanisms of Chinese remedy free and easy wanderer (FAEW) on PTSD. We used a reverse pharmacology approach combining clinical data to search for mechanisms of PTSD with subsequent in vitro verification and bioinformatics techniques as follows: (1) by analyzing microarray-based …

0301 basic medicineDrugmedicine.medical_specialtypharmacognosyMicroarraymedia_common.quotation_subjectPharmacologyNF-κB03 medical and health scienceschemistry.chemical_compoundIn vivofree and easy wanderermedicinePharmacology (medical)PsychiatryMode of actionOriginal Researchmedia_commonPharmacologyFluoxetineReverse pharmacologybusiness.industryPaeoniflorin030104 developmental biologychemistryinflammationposttraumatic stress disorderAntidepressantbusinessmedicine.drugFrontiers in Pharmacology
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New Alkenylresorcinols with Cytotoxic and Antimicrobial Activities from the Leaves of Embelia schimperi.

2020

AbstractA phytochemical study of the methanol extract of the leaves of Embelia schimperi resulted in the isolation of three new alkenylresorcinols, 1 – 3, together with the known analogs 4 – 7. Their structures were established by a combination of spectroscopic techniques. Compounds 1 – 7 exhibited moderate cytotoxic activity against human cervical cancer cells HeLa-S3 and more pronounced antimicrobial properties towards bacteria and filamentous fungi. The present study falls into an ongoing research project on the characterization of bioactive phenolic lipids from plants of the family Primulaceae.

EmbeliaPhytochemicalsPharmaceutical ScienceEmbelia01 natural sciencesAnalytical ChemistryAnti-Infective AgentsDrug DiscoveryCytotoxic T cellHumansCytotoxicityPharmacologyTraditional medicinebiology010405 organic chemistryChemistryPlant ExtractsOrganic ChemistryIsolation (microbiology)biology.organism_classificationAntimicrobial0104 chemical sciencesPlant Leaves010404 medicinal & biomolecular chemistryPrimulaceaeComplementary and alternative medicinePhytochemicalMolecular MedicineBacteriaPlanta medica
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Applicability of a single‐use bioreactor compared to a glass bioreactor for the fermentation of filamentous fungi and evaluation of the reproducibili…

2021

Abstract The implementation of single‐use technologies offers several major advantages, e.g. prevention of cross‐contamination, especially when spore‐forming microorganisms are present. This study investigated the application of a single‐use bioreactor in batch fermentation of filamentous fungus Penicillium sp. (IBWF 040‐09) from the Institute of Biotechnology and Drug Research (IBWF), which is capable of intracellular production of a protease inhibitor against parasitic proteases as a secondary metabolite. Several modifications to the SU bioreactor were suggested in this study to allow the fermentation in which the fungus forms pellets. Simultaneously, fermentations in conventional glass b…

0106 biological sciencesEnvironmental Engineeringsingle‐use bioreactorMicroorganismPenicillium spBioengineeringSecondary metabolite01 natural sciencesprotease inhibitor03 medical and health sciences010608 biotechnologyPelletmedicineBioreactorFood sciencefermentationResearch Articles030304 developmental biology0303 health sciencesbiologyChemistrytechnology industry and agricultureSubstrate (chemistry)biology.organism_classificationequipment and suppliespelletsSingle-use bioreactorPenicilliumFermentationTP248.13-248.65Biotechnologymedicine.drugResearch ArticleEngineering in Life Sciences
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Terphenyl Derivatives from Allantophomopsis lycopodina.

2016

Three secondary fungal metabolites 1–3 with a benzo[b]naphtho[2,1-d]furan skeleton were isolated from submerged cultures of the ascomycete Allantophomopsis lycopodina. The NMR-based structure elucidation was challenging due to a low H/C ratio of only 0.64 and 0.68, respectively. NMR measurements in two different solvents and the use of NMR experiments such as HSQC-TOCSY and LR-HSQMBC proved to be helpful in this respect. The proposed structures obtained from the comprehensive analysis of the NMR data were verified by comparison of recorded and computed NMR chemical shifts from quantum chemical calculations of several constitutional isomers and were further analyzed with the aid of the DP4 a…

StereochemistryPharmaceutical ScienceAllantophomopsis lycopodina010402 general chemistry01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundAscomycotaComputational chemistryTerphenylFuranTerphenyl CompoundsDrug DiscoveryStructural isomerNuclear Magnetic Resonance BiomolecularPharmacologyQuantum chemicalMolecular Structure010405 organic chemistryChemical shiftOrganic ChemistryNmr data0104 chemical sciencesComplementary and alternative medicinechemistryMolecular MedicineJournal of natural products
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Discovery of an Extended Austinoid Biosynthetic Pathway in Aspergillus calidoustus

2017

Filamentous fungi produce a wide range of natural products that are commonly used in various industrial contexts (e.g., pharmaceuticals and insecticides). Meroterpenoids are natural products of interest because of their various biological activities. Among the meroterpenoids, there is a group of insecticidal compounds known as the austinoids. These compounds have also been studied because of their intriguing spiro-lactone ring formation along with various modifications. Here, we present an extension of the original austinol/dehydroaustinol biosynthesis pathway from Aspergillus nidulans in the recently identified filamentous fungus Aspergillus calidoustus. Besides the discovery and elucidati…

InsecticidesGenes Fungal010402 general chemistry01 natural sciencesBiochemistryAspergillus nidulansMicrobiologyTerpenechemistry.chemical_compoundBiosynthesisAspergillus nidulansPolyketide synthaseGeneAspergillusAspergillus calidoustusbiologyTerpenes010405 organic chemistryGeneral Medicinebiology.organism_classificationBiosynthetic Pathways0104 chemical sciencesAspergilluschemistryBiochemistryPolyketidesbiology.proteinMolecular MedicineDimerizationPolyketide SynthasesMetabolic Networks and PathwaysBiosynthetic genesACS Chemical Biology
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Hog1p activation by marasmic acid through inhibition of the histidine kinase Sln1p

2016

BACKGROUND The histidine kinase (HK) MoHik1p within the high-osmolarity glycerol (HOG) pathway is known to be the target of the fungicide fludioxonil. Treatment of the fungus with fludioxonil causes an uncontrolled hyperactivation of the pathway and cell death. In this study, we used a target-based in vivo test system with mutant strains of the rice blast fungus Magnaporthe oryzae to search for new fungicidal compounds having various target locations within the HOG pathway. Mutants with inactivated HOG signalling are resistant to fungicides having the target located in the HOG pathway. RESULTS The HK MoSln1p was identified as being involved in the new antifungal mode of action of marasmic a…

0301 basic medicineFungal proteinMagnaporthebiologyMutantHistidine kinaseGeneral MedicineFludioxonilbiology.organism_classificationMicrobiology03 medical and health sciencesMetabolic pathway030104 developmental biologyBiochemistryInsect SciencePhosphorylationMode of actionAgronomy and Crop SciencePest Management Science
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Promoter Activation in Dhfq Mutants as an Efficient Tool for Specialized Metabolite Production Enabling Direct Bioactivity Testing

2019

Abstract Natural products (NPs) from microorganisms have been important sources for discovering new therapeutic and chemical entities. While their corresponding biosynthetic gene clusters (BGCs) can be easily identified by gene‐sequence‐similarity‐based bioinformatics strategies, the actual access to these NPs for structure elucidation and bioactivity testing remains difficult. Deletion of the gene encoding the RNA chaperone, Hfq, results in strains losing the production of most NPs. By exchanging the native promoter of a desired BGC against an inducible promoter in Δhfq mutants, almost exclusive production of the corresponding NP from the targeted BGC in Photorhabdus, Xenorhabdus and Pseud…

bioactivity testingnatural productsMetaboliteMutantPeptide SynthetasesXenorhabdus010402 general chemistry01 natural sciencesCatalysisBiosynthesis | Very Important Paperchemistry.chemical_compoundddc:570RNA chaperoneHumansMetabolomicsGeneResearch ArticlesBiological Productsbiology010405 organic chemistryPseudomonastechnology industry and agricultureGeneral MedicineGeneral Chemistrybiology.organism_classification0104 chemical sciencesBiosynthetic PathwayseasyPACIdchemistryBiochemistryddc:540proteobacteriaPhotorhabdussimplified productionResearch Article
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The Creolophins: A Family of Linear Triquinanes fromCreolophus cirrhatus (Basidiomycete)

2007

Complicatic acid and five novel linear triquinanes were isolated from mycelial cultures of Creolophus cirrhatus. The creolophins A, C, D, and E represent a novel type of highly oxidized triquinane sesquiterpenoids. Whereas those compounds with a secondary alcohol moiety in ring A are stable, the exomethylene ketone creolophin E (5) partly dimerized during workup to form the decacyclic 1,4-dioxepin-6-one neocreolophin (6). Compounds 5 and 6 display cytotoxic activities against several tumor cell lines.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

chemistry.chemical_classificationKetoneStereochemistryOrganic ChemistryAlcoholTumor cellsNuclear magnetic resonance spectroscopyRing (chemistry)Terpenoidchemistry.chemical_compoundchemistryCreolophus cirrhatusMoietyPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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CCDC 962065: Experimental Crystal Structure Determination

2016

Related Article: Louis P. Sandjo, Eckhard Thines, Till Opatz and Anja Schüffler|2014|Beilstein J.Org.Chem.|10|251|doi:10.3762/bjoc.10.20

Space GroupCrystallographyCrystal SystemCrystal Structure(2E4E)-5-((5S6S8R)-5-hydroxy-268-trimethyl-5678-tetrahydronaphthalen-1-yl)penta-24-dienoic acidCell ParametersExperimental 3D Coordinates
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CCDC 962066: Experimental Crystal Structure Determination

2017

Related Article: Louis P. Sandjo, Eckhard Thines, Till Opatz and Anja Schüffler|2014|Beilstein J.Org.Chem.|10|251|doi:10.3762/bjoc.10.20

Space GroupCrystallographyCrystal SystemCrystal Structure(2E4E)-5-[(1S2S4aR6R8R8aS)-6-hydroxy-268-trimethyl-124a56788a-octahydronaphthalen-1-yl]penta-24-dienoic acidCell ParametersExperimental 3D Coordinates
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CCDC 2081480: Experimental Crystal Structure Determination

2022

Related Article: Leander Geske, Ulrich Kauhl, Mohamed Saeed, Anja Schüffler, Eckhard Thines, Thomas Efferth, Till Opatz|2021|Molecules|26|3224|doi:10.3390/molecules26113224

Space GroupCrystallographyCrystal SystemCrystal Structure5-[2-(3-hydroxyphenyl)ethyl]-4-[(4-hydroxyphenyl)methyl]benzene-13-diolCell ParametersExperimental 3D Coordinates
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